Medical Device Manufacturer · US , Byron Center , MI

Transcorp, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2010

Total

Cleared

Denied

Transcorp, Inc. has 4 FDA 510(k) cleared medical devices. Based in Byron Center, US.

Historical record: 4 cleared submissions from 2010 to 2013. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Transcorp, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Transcorp, Inc.

4 devices

1-4 of 4